ID
29073
Beschrijving
Study ID: 101468/249 Clinical Study ID: 101468/249 Study Title: A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363857 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: N/A Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Restless Legs Syndrome; Restless Legs Syndrome (RLS)
Trefwoorden
Versies (1)
- 23-02-18 23-02-18 -
Houder van rechten
GlaxoSmithKline (GSK)
Geüploaded op
23 februari 2018
DOI
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Licentie
Creative Commons BY-NC 3.0
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Clinical Study, Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS), Study ID: 101468/249, NCT00363857
Abnormal findings at the Screening Visit
- StudyEvent: ODM
Beschrijving
Electrocardiogram (12 lead)
Alias
- UMLS CUI-1
- C0430456
Beschrijving
Dato of ECG
Datatype
date
Alias
- UMLS CUI [1]
- C2826640
Beschrijving
If ’Yes’, please record details in the Baseline Signs and Symptoms and/or SAE section at the back of this book and exclude the patient from the study.
Datatype
integer
Alias
- UMLS CUI [1]
- C0522055
Beschrijving
Laboratory evaluation
Alias
- UMLS CUI-1
- C0022885
Beschrijving
Date of sample
Datatype
date
Alias
- UMLS CUI [1]
- C1302413
Beschrijving
If ‘Yes’, please record the findings and/or diagnosis in the Baseline Signs and Symptoms and/or SAE section at the back of this book and exclude the patient from the study.
Datatype
integer
Alias
- UMLS CUI [1]
- C1853129
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Abnormal findings at the Screening Visit
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])